digoxin

Generic: digoxin

Labeler: hikma pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name digoxin
Generic Name digoxin
Labeler hikma pharmaceuticals usa inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

digoxin 250 ug/1

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0143-1241
Product ID 0143-1241_935f4e33-109c-448c-822c-530145dbbc05
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077002
Listing Expiration 2026-12-31
Marketing Start 2007-10-30

Pharmacologic Class

Established (EPC)
cardiac glycoside [epc]
Chemical Structure
cardiac glycosides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01431241
Hyphenated Format 0143-1241

Supplemental Identifiers

RxCUI
197604 197606
UPC
0301431240103 0301431241100
UNII
73K4184T59
NUI
N0000175568 M0003451

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name digoxin (source: ndc)
Generic Name digoxin (source: ndc)
Application Number ANDA077002 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 ug/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (0143-1241-01)
  • 1000 TABLET in 1 BOTTLE, PLASTIC (0143-1241-10)
source: ndc

Packages (2)

Ingredients (1)

digoxin (250 ug/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "935f4e33-109c-448c-822c-530145dbbc05", "openfda": {"nui": ["N0000175568", "M0003451"], "upc": ["0301431240103", "0301431241100"], "unii": ["73K4184T59"], "rxcui": ["197604", "197606"], "spl_set_id": ["41c16cff-b03e-405e-a617-d6f45d3ce2bd"], "pharm_class_cs": ["Cardiac Glycosides [CS]"], "pharm_class_epc": ["Cardiac Glycoside [EPC]"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0143-1241-01)", "package_ndc": "0143-1241-01", "marketing_start_date": "20071030"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (0143-1241-10)", "package_ndc": "0143-1241-10", "marketing_start_date": "20071030"}], "brand_name": "Digoxin", "product_id": "0143-1241_935f4e33-109c-448c-822c-530145dbbc05", "dosage_form": "TABLET", "pharm_class": ["Cardiac Glycoside [EPC]", "Cardiac Glycosides [CS]"], "product_ndc": "0143-1241", "generic_name": "Digoxin", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Digoxin", "active_ingredients": [{"name": "DIGOXIN", "strength": "250 ug/1"}], "application_number": "ANDA077002", "marketing_category": "ANDA", "marketing_start_date": "20071030", "listing_expiration_date": "20261231"}